Li Lianqin, Shoji Wataru, Takano Hirohisa, Nishimura Noriko, Aoki Yasunobu, Takahashi Ryoya, Goto Sataro, Kaifu Tomonori, Takai Toshiyuki, Obinata Masuo
Department of Cell Biology, Institute of Development, Aging, and Cancer, Tohoku University, 4-1 Seriyo-machi, Aoba-ku, Sendai 980-8575, Japan.
Biochem Biophys Res Commun. 2007 Apr 13;355(3):715-21. doi: 10.1016/j.bbrc.2007.02.022. Epub 2007 Feb 12.
MER5 (also called peroxiredoxin III, PrxIII) is a member of peroxiredoxin family that has antioxidant activity. The present study was performed to investigate its in vivo function using MER5 knockout mice. MER5 knockout mice were born in normal frequency and could grow to maturity, but we found that intracellular ROS levels are significantly higher in the macrophages of the knockout mice. We examined roles of MER5 function for the oxidative stress responses by intratracheal inoculation of lipopolysaccharide (LPS) to the mice. Lung inflammation such as inflammatory cell infiltration and airway wall thickening was more severely detected in the knockout mice. At the same time, oxidative damage on DNA and proteins was more strongly detected in lung tissues of the knockout mice, including 8-hydroxy-2'-deoxyguanosine (8-OHdG) formation and protein carbonylation. The degrees of lung inflammation and oxidative damage were positively related with LPS doses. Our results indicate that MER5 knockout mice accumulated higher intracellular ROS levels, which cause LPS-induced lung injury more severely, and thus, suggested that MER5 acts as an important scavenger of reactive oxygen species (ROS) under oxidative stress.
MER5(也称为过氧化物酶III,PrxIII)是具有抗氧化活性的过氧化物酶家族成员。本研究旨在使用MER5基因敲除小鼠来研究其体内功能。MER5基因敲除小鼠出生频率正常,能够生长至成熟,但我们发现敲除小鼠巨噬细胞内的活性氧水平显著更高。我们通过向小鼠气管内接种脂多糖(LPS)来研究MER5功能在氧化应激反应中的作用。在敲除小鼠中更严重地检测到了肺部炎症,如炎症细胞浸润和气道壁增厚。同时,在敲除小鼠的肺组织中更强烈地检测到了对DNA和蛋白质的氧化损伤,包括8-羟基-2'-脱氧鸟苷(8-OHdG)的形成和蛋白质羰基化。肺部炎症和氧化损伤的程度与LPS剂量呈正相关。我们的结果表明,MER5基因敲除小鼠积累了更高的细胞内活性氧水平,这更严重地导致了LPS诱导的肺损伤,因此,提示MER5在氧化应激下作为活性氧(ROS)的重要清除剂发挥作用。